Robert the Pilegrim said:In post 652 of this thread I briefly outlined the evidence for evolution and against the belief that "evolutionist... just throw in millions of years."
http://www.christianforums.com/showthread.php?p=10778623&postcount=652
One of the links I provided was the following:
http://www.talkorigins.org/faqs/molgen/
One of the examples given is the case of GLO deficency.
Very briefly, monkeys, apes and humans share a non-functional gene, and the commonality of the errors that accumulated in that gene is greater for species that appear physiologically to be more closely related, i.e. the errors look just as they would if we evolved from a common ancestor.
Somewhat less briefly:
The production of vitamin C is controlled by several genes, but one in particular produces an enzyme, L-gulonolactone oxidase (GLO), that is required for the last step in the production of vitamin C.
All species of mammals that have been examined* have, as is expected, a nearly identical gene for producing GLO in essentially the same spot on the chromosomes.
(*It is fairly expensive to do this kind of work so not every of the thousands of species of mammals have been examined)
But monkeys, apes and humans don't produce GLO, we don't produce our own vitamin C.
An examination of DNA from a human, a chimpanzee, a gorilla, an orangutang and an old world monkey demonstrated that all had the same mutation in the start portion of the gene that produced GLO.
A mutation in the start portion of a gene will generally prevent that gene from being activated at all. In contrast a mutation in the middle of a gene is likely to cause the gene to misbehave, in this case it might create an enzyme that would mal-function rendering the vitamin-C percurser useless, or attacking some other useful bio-chemical, thus a mutation in the middle of the gene will tend to disappear from the gene pool altogether while "merely" stopping the gene in circumstances where there is plenty of vitamin C available from food will allow that mutation to be passed on, and for that non-functional gene to accumulate mutations.
By examining the physiology of the great apes, orangutangs had been placed farthest from humans, then gorillas, with chimpanzees closest and of course monkeys are even farther than orangutangs. In examining the DNA (in particular the gene dealing with vitamin C but other parts as well) it was found that humans share many of the same mutations that chimpanzees have, and that we share fewer with gorillas, fewer still with orangutangs and fewest with the monkey.
Which is what we expect if we evolved from a common ancestor. For some period of time mutations would accumulate which we would share, then as species branched off the mutations they accumulated would be unique to them, while our branch would continue to accumulate mutations unique to ours.
Again, the point here is that we share a non-functional gene and that the differences in the mutations that accumulated in each of the species are what we would expect if descended from a common ancestor in exactly the manner that was predicted by looking at the physiology of the species.
Bla Bla Bla like a said before so what if it is happening now thats great its just infomation of what is happening now and you make it appear to be evolution. mass infomation no conformation. talk origans is the same as i get here, a lot of neat things that happen in our world. were are all the transitional forms on earth. if its random mutation then their would be a lot of species with extra stuff for future use in another species. everything is fullyformed and functional. unless we all evolve at the same time. and so slowly we dont even catch any of it.
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